| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5213210 | Tetrahedron | 2016 | 7 Pages |
Abstract
Novel [1]benzothien-2-yl fulgides have been synthesized. Under irradiation the compounds with R1=H undergo reversible Z/E-photoisomerization, the compound with a methyl group (R1=Me) at the methylidene bridge rearranges into the thermally stable colored ring-closed isomer.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
![Photochromism of novel [1]benzothien-2-yl fulgides](/preview/png/5213210.png "First Page Preview: Photochromism of novel [1]benzothien-2-yl fulgides")
Authors
Sofiya Yu. Zmeeva, Vladimir P. Rybalkin, Lidiya L. Popova, Valerii V. Tkachev, Yurii V. Revinskii, Karina S. Tikhomirova, Andrey G. Starikov, Alexander D. Dubonosov, Vladimir A. Bren, Sergey M. Aldoshin, Vladimir I. Minkin,